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Showing metabocard for Diisopropyl sulfide (HMDB0029579)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 17:31:15 UTC
Update Date2023-02-21 17:18:50 UTC
HMDB IDHMDB0029579
Secondary Accession Numbers
  • HMDB29579
Metabolite Identification
Common NameDiisopropyl sulfide
DescriptionDiisopropyl sulfide, also known as 2,2'-thiobis-propane, belongs to the class of organic compounds known as dialkylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two alkyl groups. Diisopropyl sulfide is possibly neutral. Diisopropyl sulfide is a garlic, sulfury, and vegetable tasting compound.
Structure
Data?1676999930
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0029579 (Diisopropyl sulfide)


  Mrv1652305271900092D          

  7  6  0  0  0  0            999 V2000
   -1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  5  2  1  0  0  0  0
  6  3  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  7  6  1  0  0  0  0
M  END
Download

3D MOL for HMDB0029579 (Diisopropyl sulfide)

HMDB0029579
     RDKit          3D
Diisopropyl sulfide
 21 20  0  0  0  0  0  0  0  0999 V2000
   -1.5537    1.2201    0.2403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2871   -0.2555    0.3083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6172   -0.9764    0.1692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1959   -0.8467   -0.9906 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.5039   -0.3045   -0.8062 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6354    1.1412   -0.4061 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3014   -1.1235    0.1662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6441    1.4475    0.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2393    1.6694    1.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0604    1.7237   -0.6040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8605   -0.5561    1.2972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0159   -0.7715   -0.8572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3453   -0.5142    0.8726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4987   -2.0661    0.3352 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9936   -0.3967   -1.8076 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2168    1.3436    0.6060 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2603    1.8182   -1.1859 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7335    1.3429   -0.3241 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3633   -1.1330   -0.1844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9882   -2.1732    0.2399 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3217   -0.5891    1.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  1  8  1  0
  1  9  1  0
  1 10  1  0
  2 11  1  0
  3 12  1  0
  3 13  1  0
  3 14  1  0
  5 15  1  0
  6 16  1  0
  6 17  1  0
  6 18  1  0
  7 19  1  0
  7 20  1  0
  7 21  1  0
M  END
Download

3D SDF for HMDB0029579 (Diisopropyl sulfide)


  Mrv1652305271900092D          

  7  6  0  0  0  0            999 V2000
   -1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  5  2  1  0  0  0  0
  6  3  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  7  6  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0029579

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)SC(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C6H14S/c1-5(2)7-6(3)4/h5-6H,1-4H3

> <INCHI_KEY>
XYWDPYKBIRQXQS-UHFFFAOYSA-N

> <FORMULA>
C6H14S

> <MOLECULAR_WEIGHT>
118.24

> <EXACT_MASS>
118.081621138

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
21

> <JCHEM_AVERAGE_POLARIZABILITY>
14.894019049112703

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(propan-2-ylsulfanyl)propane

> <ALOGPS_LOGP>
3.01

> <JCHEM_LOGP>
2.3552336030000003

> <ALOGPS_LOGS>
-2.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
37.423300000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.82e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,4-dimethyl-3-thiapentane

> <JCHEM_VEBER_RULE>
1

$$$$
Download

3D-SDF for HMDB0029579 (Diisopropyl sulfide)

HMDB0029579
     RDKit          3D
Diisopropyl sulfide
 21 20  0  0  0  0  0  0  0  0999 V2000
   -1.5537    1.2201    0.2403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2871   -0.2555    0.3083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6172   -0.9764    0.1692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1959   -0.8467   -0.9906 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.5039   -0.3045   -0.8062 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6354    1.1412   -0.4061 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3014   -1.1235    0.1662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6441    1.4475    0.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2393    1.6694    1.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0604    1.7237   -0.6040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8605   -0.5561    1.2972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0159   -0.7715   -0.8572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3453   -0.5142    0.8726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4987   -2.0661    0.3352 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9936   -0.3967   -1.8076 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2168    1.3436    0.6060 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2603    1.8182   -1.1859 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7335    1.3429   -0.3241 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3633   -1.1330   -0.1844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9882   -2.1732    0.2399 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3217   -0.5891    1.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  1  8  1  0
  1  9  1  0
  1 10  1  0
  2 11  1  0
  3 12  1  0
  3 13  1  0
  3 14  1  0
  5 15  1  0
  6 16  1  0
  6 17  1  0
  6 18  1  0
  7 19  1  0
  7 20  1  0
  7 21  1  0
M  END
Download

PDB for HMDB0029579 (Diisopropyl sulfide)

HEADER    PROTEIN                                 27-MAY-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-MAY-19         0                                  
HETATM    1  C   UNK     0      -2.310  -1.334   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -2.667   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.310  -1.334   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM    7  S   UNK     0       0.000   0.000   0.000  0.00  0.00           S+0
CONECT    1    5                                                            
CONECT    2    5                                                            
CONECT    3    6                                                            
CONECT    4    6                                                            
CONECT    5    1    2    7                                                  
CONECT    6    3    4    7                                                  
CONECT    7    5    6                                                       
MASTER        0    0    0    0    0    0    0    0    7    0   12    0
END
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3D PDB for HMDB0029579 (Diisopropyl sulfide)

COMPND    HMDB0029579
HETATM    1  C1  UNL     1      -1.554   1.220   0.240  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.287  -0.255   0.308  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.617  -0.976   0.169  1.00  0.00           C  
HETATM    4  S1  UNL     1      -0.196  -0.847  -0.991  1.00  0.00           S  
HETATM    5  C4  UNL     1       1.504  -0.305  -0.806  1.00  0.00           C  
HETATM    6  C5  UNL     1       1.635   1.141  -0.406  1.00  0.00           C  
HETATM    7  C6  UNL     1       2.301  -1.123   0.166  1.00  0.00           C  
HETATM    8  H1  UNL     1      -2.644   1.447   0.147  1.00  0.00           H  
HETATM    9  H2  UNL     1      -1.239   1.669   1.211  1.00  0.00           H  
HETATM   10  H3  UNL     1      -1.060   1.724  -0.604  1.00  0.00           H  
HETATM   11  H4  UNL     1      -0.860  -0.556   1.297  1.00  0.00           H  
HETATM   12  H5  UNL     1      -3.016  -0.772  -0.857  1.00  0.00           H  
HETATM   13  H6  UNL     1      -3.345  -0.514   0.873  1.00  0.00           H  
HETATM   14  H7  UNL     1      -2.499  -2.066   0.335  1.00  0.00           H  
HETATM   15  H8  UNL     1       1.994  -0.397  -1.808  1.00  0.00           H  
HETATM   16  H9  UNL     1       1.217   1.344   0.606  1.00  0.00           H  
HETATM   17  H10 UNL     1       1.260   1.818  -1.186  1.00  0.00           H  
HETATM   18  H11 UNL     1       2.733   1.343  -0.324  1.00  0.00           H  
HETATM   19  H12 UNL     1       3.363  -1.133  -0.184  1.00  0.00           H  
HETATM   20  H13 UNL     1       1.988  -2.173   0.240  1.00  0.00           H  
HETATM   21  H14 UNL     1       2.322  -0.589   1.140  1.00  0.00           H  
CONECT    1    2    8    9   10
CONECT    2    3    4   11
CONECT    3   12   13   14
CONECT    4    5
CONECT    5    6    7   15
CONECT    6   16   17   18
CONECT    7   19   20   21
END
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SMILES for HMDB0029579 (Diisopropyl sulfide)

CC(C)SC(C)C
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INCHI for HMDB0029579 (Diisopropyl sulfide)

InChI=1S/C6H14S/c1-5(2)7-6(3)4/h5-6H,1-4H3
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View in JSmolView Stereo Labels
Synonyms
ValueSource
Diisopropyl sulphideGenerator
2,2'-Thiobis-propaneHMDB
2,2'-Thiobispropane, 9ciHMDB
2,2'-ThiodipropaneHMDB
2,4-Dimethyl-3-thiapentaneHMDB
2-(Isopropylsulfanyl)propaneHMDB
Isopropyl sulfide, 8ciHMDB
Isopropyl sulphideHMDB
2-(Propan-2-ylsulphanyl)propaneHMDB
Chemical FormulaC6H14S
Average Molecular Weight118.24
Monoisotopic Molecular Weight118.081621138
IUPAC Name2-(propan-2-ylsulfanyl)propane
Traditional Name2,4-dimethyl-3-thiapentane
CAS Registry Number625-80-9
SMILES
CC(C)SC(C)C
InChI Identifier
InChI=1S/C6H14S/c1-5(2)7-6(3)4/h5-6H,1-4H3
InChI KeyXYWDPYKBIRQXQS-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as dialkylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two alkyl groups.
KingdomOrganic compounds
Super ClassOrganosulfur compounds
ClassThioethers
Sub ClassDialkylthioethers
Direct ParentDialkylthioethers
Alternative Parents
Substituents
  • Dialkylthioether
  • Sulfenyl compound
  • Hydrocarbon derivative
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effect
Organoleptic effect
Disposition
Biological locationSource
ProcessNot Available
RoleNot Available
Physical Properties
StateLiquid
Experimental Molecular Properties
PropertyValueReference
Melting Point-78.1 °CNot Available
Boiling Point120.00 to 122.00 °C. @ 760.00 mm HgThe Good Scents Company Information System
Water Solubility382.5 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP2.84Not Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.28 g/LALOGPS
logP3.01ALOGPS
logP2.36ChemAxon
logS-2.6ALOGPS
Physiological Charge0ChemAxon
Hydrogen Acceptor Count0ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area0 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity37.42 m³·mol⁻¹ChemAxon
Polarizability14.89 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+124.97531661259
DarkChem[M-H]-120.10931661259
DeepCCS[M+H]+137.27730932474
DeepCCS[M-H]-134.96730932474
DeepCCS[M-2H]-171.04830932474
DeepCCS[M+Na]+146.16830932474
AllCCS[M+H]+125.632859911
AllCCS[M+H-H2O]+121.732859911
AllCCS[M+NH4]+129.232859911
AllCCS[M+Na]+130.232859911
AllCCS[M-H]-136.332859911
AllCCS[M+Na-2H]-140.532859911
AllCCS[M+HCOO]-145.032859911

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.4.19 minutes32390414
Predicted by Siyang on May 30, 202214.7092 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20223.04 minutes32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid40.9 seconds40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid2056.7 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid568.0 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid198.8 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid351.4 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid83.0 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid560.2 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid613.2 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)128.0 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid1073.6 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid553.7 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid1227.8 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid395.6 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid298.7 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate539.1 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA533.1 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water44.8 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Diisopropyl sulfideCC(C)SC(C)C984.9Standard polar33892256
Diisopropyl sulfideCC(C)SC(C)C763.8Standard non polar33892256
Diisopropyl sulfideCC(C)SC(C)C784.3Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental GC-MSGC-MS Spectrum - Diisopropyl sulfide EI-B (Non-derivatized)splash10-01ox-9100000000-42ef19203255107e712c2017-09-12HMDB team, MONA, MassBankView Spectrum
Experimental GC-MSGC-MS Spectrum - Diisopropyl sulfide EI-B (Non-derivatized)splash10-01ox-9100000000-42ef19203255107e712c2018-05-18HMDB team, MONA, MassBankView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Diisopropyl sulfide GC-MS (Non-derivatized) - 70eV, Positivesplash10-0006-9100000000-c7fb9f5d47c4c3dea20c2016-09-22Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Diisopropyl sulfide GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Diisopropyl sulfide 10V, Positive-QTOFsplash10-014i-2900000000-93e6c963fc30022fb1462015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Diisopropyl sulfide 20V, Positive-QTOFsplash10-014i-2900000000-9cabfb654109c12a2a9a2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Diisopropyl sulfide 40V, Positive-QTOFsplash10-002f-9000000000-1cbb885ff7a2f6f94a2f2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Diisopropyl sulfide 10V, Negative-QTOFsplash10-014i-2900000000-6cae09bf33baca65c0cb2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Diisopropyl sulfide 20V, Negative-QTOFsplash10-016r-8900000000-05a2875846c221a0aede2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Diisopropyl sulfide 40V, Negative-QTOFsplash10-004i-9000000000-db8ea5717d36d9bf09f72015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Diisopropyl sulfide 10V, Positive-QTOFsplash10-014i-2900000000-0346c9ab14c9aa4ef0172021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Diisopropyl sulfide 20V, Positive-QTOFsplash10-004i-9300000000-99057670fb0f598527202021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Diisopropyl sulfide 40V, Positive-QTOFsplash10-06vi-9000000000-15c3112e42424d5e98132021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Diisopropyl sulfide 10V, Negative-QTOFsplash10-014i-2900000000-4f027d081c809fc567052021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Diisopropyl sulfide 20V, Negative-QTOFsplash10-004i-9000000000-8f8287bbd49c4be555dc2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Diisopropyl sulfide 40V, Negative-QTOFsplash10-00b9-9000000000-20b5eb569e3d041256fc2021-09-23Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)2023-02-03FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-03FELIX labView Spectrum
Biological Properties
Cellular Locations
  • Membrane
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB000735
KNApSAcK IDNot Available
Chemspider ID11761
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound12264
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1042561
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .